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Therapeutic efficacy of monoclonal antibodies and antivirals against SARS-CoV-2 Omicron BA.1 in Syrian hamsters.
Uraki, Ryuta; Kiso, Maki; Imai, Masaki; Yamayoshi, Seiya; Ito, Mutsumi; Fujisaki, Seiichiro; Takashita, Emi; Ujie, Michiko; Furusawa, Yuri; Yasuhara, Atsuhiro; Iwatsuki-Horimoto, Kiyoko; Sakai-Tagawa, Yuko; Watanabe, Shinji; Hasegawa, Hideki; Kawaoka, Yoshihiro.
  • Uraki R; Division of Virology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
  • Kiso M; The Research Center for Global Viral Diseases, National Center for Global Health and Medicine Research Institute, Tokyo, Japan.
  • Imai M; Division of Virology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
  • Yamayoshi S; Division of Virology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
  • Ito M; The Research Center for Global Viral Diseases, National Center for Global Health and Medicine Research Institute, Tokyo, Japan.
  • Fujisaki S; Division of Virology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
  • Takashita E; The Research Center for Global Viral Diseases, National Center for Global Health and Medicine Research Institute, Tokyo, Japan.
  • Ujie M; Division of Virology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
  • Furusawa Y; Center for Influenza and Respiratory Virus Research, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.
  • Yasuhara A; Center for Influenza and Respiratory Virus Research, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.
  • Iwatsuki-Horimoto K; Division of Virology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
  • Sakai-Tagawa Y; The Research Center for Global Viral Diseases, National Center for Global Health and Medicine Research Institute, Tokyo, Japan.
  • Watanabe S; Division of Virology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
  • Hasegawa H; The Research Center for Global Viral Diseases, National Center for Global Health and Medicine Research Institute, Tokyo, Japan.
  • Kawaoka Y; Division of Virology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
Nat Microbiol ; 7(8): 1252-1258, 2022 08.
Article in English | MEDLINE | ID: covidwho-1890192
ABSTRACT
The spike protein of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the major antigen stimulating the host's protective immune response. Here we assessed the efficacy of therapeutic monoclonal antibodies (mAbs) against Omicron variant (B.1.1.529) sublineage BA.1 variants in Syrian hamsters. Of the FDA-approved therapeutic mAbs tested (that is, REGN10987/REGN10933, COV2-2196/COV2-2130 and S309), only COV2-2196/COV2-2130 efficiently inhibited BA.1 replication in the lungs of hamsters, and this effect was diminished against a BA.1.1 variant possessing the S-R346K substitution. In addition, treatment of BA.1-infected hamsters with molnupiravir (a SARS-CoV-2 RNA-dependent RNA polymerase inhibitor) or S-217622 (a SARS-CoV-2 protease inhibitor) strongly reduced virus replication in the lungs. These findings suggest that the use of therapeutic mAbs in Omicron-infected patients should be carefully considered due to mutations that affect efficacy, and demonstrate that the antiviral compounds molnupiravir and S-217622 are effective against Omicron BA.1 variants.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Drug Treatment Topics: Variants Limits: Animals / Humans Language: English Journal: Nat Microbiol Year: 2022 Document Type: Article Affiliation country: S41564-022-01170-4

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Drug Treatment Topics: Variants Limits: Animals / Humans Language: English Journal: Nat Microbiol Year: 2022 Document Type: Article Affiliation country: S41564-022-01170-4